| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:15469264-15469615 | Common:2; Rare:91 | ||||
| chr9:15469938-15470224 | Rare:90 | ||||
| chr9:15479612-15479799 | Common:1; Rare:59 | ||||
| chr9:15486004-15486233 | Rare:67 | ||||
| chr9:15486820-15487114 | Common:3; Rare:82 | ||||
| chr9:16726808-16726821 | Rare:3 | ||||
| chr9:19102442-19102531 | Common:1; Rare:40 | ||||
| chr9:19378368-19378939 | Common:1; Rare:169 | ||||
| chr9:20620786-20621039 | Common:2; Rare:84 | ||||
| chr9:25677485-25677721 | Common:2; Rare:114 | ||||
| chr9:28491401-28491435 | Rare:5 | ||||
| chr9:32550811-32551156 | Common:1; Rare:137; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:33166618-33166656 | Rare:10 | ||||
| chr9:34380790-34380930 | Common:1; Rare:51 | ||||
| chr9:34809993-34810053 | Common:1; Rare:26 |